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Myelotec, Inc. recalls Myelotec Video Guided Catheters, REF 2010 3.0 mm OD x 30 Cm Working Length, Two 1.3mm Working Channels
Recalled August 9, 2017 · FDA recall Z-2779-2017 · Myelotec
Hazard
Obstructed/blocked port from defective VGC Access Port Body component. · FDA Class II
Units
2980 units
Sold at
Worldwide Distribution - US Distribution to the states of : CA, FL, KY, MN, and NJ ., and to the countries of : Brazil, Iran, Kuwait, Malaysia, Singapore, South Korea, Taiwan, and Turkey
Description
Obstructed/blocked port from defective VGC Access Port Body component.
Product
Myelotec Video Guided Catheters, REF 2010 3.0 mm OD x 30 Cm Working Length, Two 1.3mm Working Channels
Manufacturer(s)
Myelotec, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →